Department of Epidemiology and Prevention, Wake Forest University Public Health Sciences, Winston-Salem, NC; Division of Gastroenterology and Hepatology, Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, NC.
Division of Allergy and Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
J Allergy Clin Immunol. 2018 Feb;141(2):632-637.e5. doi: 10.1016/j.jaci.2017.07.010. Epub 2017 Oct 10.
Although eosinophilic esophagitis (EoE) is associated with certain gene variants, the rapidly increasing incidence of EoE suggests that environmental factors contribute to disease development.
We tested for gene-environment interaction between EoE-predisposing polymorphisms (within TSLP, LOC283710/KLF13, CAPN14, CCL26, and TGFB) and implicated early-life factors (antibiotic use in infancy, cesarean delivery, breast-feeding, neonatal intensive care unit [NICU] admission, and absence of pets in the home).
We conducted a case-control study using hospital-based cases (n = 127) and control subjects representative of the hospital catchment area (n = 121). We computed case-only interaction tests and in secondary analyses evaluated the combined and independent effects of genotype and environmental factors on the risk of EoE.
Case-only analyses identified interactions between rs6736278 (CAPN14) and breast-feeding (P = .02) and rs17815905 (LOC283710/KLF13) and NICU admission (P = .02) but not with any of the factors examined. Case-control analyses suggested that disease risk might be modifiable in subjects with certain gene variants. In particular, breast-feeding in those with the susceptibility gene variant at rs6736278 (CAPN14) reduced the risk of EoE (adjusted odds ratio, 0.08; 95% CI, 0.01-0.59). Admission to the NICU in those without the susceptibility gene variant at rs17815905 (LOC283710/KLF13) significantly increased the risk of having disease (adjusted odds ratio, 4.83; 95% CI, 1.49-15.66).
The interplay of gene (CAPN14 and LOC283710/KLF13) and early-life environment factors (breast-feeding and NICU admission) might contribute to EoE susceptibility.
虽然嗜酸性食管炎(EoE)与某些基因变异有关,但 EoE 的发病率迅速上升表明环境因素有助于疾病的发展。
我们检测了 EoE 易感多态性(TSLP 内、LOC283710/KLF13、CAPN14、CCL26 和 TGFB)与潜在的生命早期因素(婴儿期使用抗生素、剖腹产、母乳喂养、新生儿重症监护病房 [NICU] 入院和家中无宠物)之间的基因-环境相互作用。
我们使用基于医院的病例(n=127)和代表医院集水区的对照受试者(n=121)进行了病例对照研究。我们计算了病例仅交互检验,并在二次分析中评估了基因型和环境因素对 EoE 风险的联合和独立影响。
病例仅分析确定了 rs6736278(CAPN14)与母乳喂养之间的相互作用(P=0.02)和 rs17815905(LOC283710/KLF13)与 NICU 入院之间的相互作用(P=0.02),但与检查的任何因素都没有。病例对照分析表明,在某些基因变异的受试者中,疾病风险可能是可改变的。特别是,在 rs6736278(CAPN14)易感基因变异的受试者中进行母乳喂养可降低 EoE 的风险(调整后的优势比,0.08;95%CI,0.01-0.59)。在没有 rs17815905(LOC283710/KLF13)易感基因变异的 NICU 入院的受试者中,患病风险显著增加(调整后的优势比,4.83;95%CI,1.49-15.66)。
基因(CAPN14 和 LOC283710/KLF13)和生命早期环境因素(母乳喂养和 NICU 入院)的相互作用可能导致 EoE 的易感性。